Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies.

Hui, Lisa; Ellis, Katie; Mayen, Dora; Pertile, Mark D; Reimers, Rebecca; Sun, Luming; Vermeesch, Joris; Vora, Neeta L; Chitty, Lyn S

Hui, Lisa; Ellis, Katie; Mayen, Dora; Pertile, Mark D; Reimers, Rebecca; Sun, Luming; Vermeesch, Joris; Vora, Neeta L; Chitty, Lyn S.

Afiliación

Hui L; Department of Obstetrics and Gynaecology, University of Melbourne, Parkville, Victoria, Australia.
Ellis K; Reproductive Epidemiology Group, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Mayen D; Department of Perinatal Medicine, Mercy Hospital for Women, Heidelberg, Victoria, Australia.
Pertile MD; Department of Obstetrics and Gynaecology, Northern Health, Epping, Victoria, Australia.
Reimers R; Illumina ANZ, Sydney, New South Wales, Australia.
Sun L; Genetics Clinic, Hospital Angeles Lomas, Estado de Mexico, Mexico.
Vermeesch J; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Parkville, Victoria, Australia.
Vora NL; San Diego Perinatal Center, Rady Children's Hospital, San Diego, California, USA.
Chitty LS; Scripps Research Institute, La Jolla, California, USA.

Prenat Diagn ; 43(7): 814-828, 2023 06.

Article en En | MEDLINE | ID: mdl-37076973

Asunto(s)

Trastornos de los Cromosomas; Diagnóstico Prenatal; Embarazo; Femenino; Humanos; Trastornos de los Cromosomas/diagnóstico; Atención Prenatal

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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Trastornos de los Cromosomas Tipo de estudio: Diagnostic_studies Idioma: En Revista: Prenat Diagn Año: 2023 Tipo del documento: Article

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